Screening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting.
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Screening of WT1 mutations in exon 8 and 9 in children with steroid resistant nephrotic syndrome from a single centre and establishment of a rapid screening assay using high-resolution melting analysis in a clinical setting.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
@zh-my
2017年学术文章
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2017年學術文章
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2017年學術文章
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2017年學術文章
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name
Screening of WT1 mutations in ...... nalysis in a clinical setting.
@ast
Screening of WT1 mutations in ...... nalysis in a clinical setting.
@en
type
label
Screening of WT1 mutations in ...... nalysis in a clinical setting.
@ast
Screening of WT1 mutations in ...... nalysis in a clinical setting.
@en
prefLabel
Screening of WT1 mutations in ...... nalysis in a clinical setting.
@ast
Screening of WT1 mutations in ...... nalysis in a clinical setting.
@en
P2093
P2860
P1433
P1476
Screening of WT1 mutations in ...... nalysis in a clinical setting.
@en
P2093
Ambily Vasudevan
Anil Vasudevan
Annes Siji
Shilpa Ravindran
P2860
P2888
P356
10.1186/S12881-016-0362-7
P577
2017-01-10T00:00:00Z
P6179
1053469164